Zobrazeno 1 - 10
of 56
pro vyhledávání: '"S, Kafert"'
Autor:
J. Siefert, K. H. Hillebrandt, S. Moosburner, P. Podrabsky, D. Geisel, T. Denecke, J. K. Unger, B. Sawitzki, S. Gül-Klein, S. Lippert, P. Tang, A. Reutzel-Selke, M. H. Morgul, A. W. Reske, S. Kafert-Kasting, W. Rüdinger, J. Oetvoes, J. Pratschke, I. M. Sauer, N. Raschzok
Publikováno v:
Cell Transplantation, Vol 28 (2019)
Hepatocyte transplantation (HcTx) is a promising approach for the treatment of metabolic diseases in newborns and children. The most common application route is the portal vein, which is difficult to access in the newborn. Transfemoral access to the
Externí odkaz:
https://doaj.org/article/d1df8d6f4c824276aaef04aa34673a8d
Autor:
I.M. Sauer, S Kafert-Kasting, J K Unger, Safak Gül-Klein, P Podrabsky, Dominik Geisel, Karl H. Hillebrandt, Timm Denecke, Anja Reutzel-Selke, Peter Tang, Simon Moosburner, A W Reske, Nathanael Raschzok, W Rüdinger, J Oetvoes, J Siefert, Johann Pratschke, S Lippert, M H Morgul, Birgit Sawitzki
Publikováno v:
Cell Transplantation
Cell Transplantation, Vol 28 (2019)
Cell Transplantation, Vol 28 (2019)
Hepatocyte transplantation (HcTx) is a promising approach for the treatment of metabolic diseases in newborns and children. The most common application route is the portal vein, which is difficult to access in the newborn. Transfemoral access to the
Autor:
S. Koenig, Q. Yuan, P. Krause, H. Christiansen, M. Rave-Fraenk, S. Kafert-Kasting, H. Kriegbaum, A. Schneider, M. Ott, J. Meyburg
Publikováno v:
Cell Transplantation, Vol 20 (2011)
Hepatocyte transplantation is regarded as a promising option to correct hereditary metabolic liver disease. This study describes a novel method involving regional transient portal ischemia (RTPI) in combination with hepatic irradiation (IR) as a prep
Externí odkaz:
https://doaj.org/article/a0323320cdb448b29c27408abe384b2a
Autor:
S. Kafert-Kasting, M. Barthold, A. L. Perrier, C. Priesner, Michael Ott, Jochen Meyburg, Andrea Schneider, H. Kriegbaum, Masoumeh Attaran
Publikováno v:
Archives of Toxicology. 86:1413-1422
Liver cell transplantation (LCT) is considered a new therapeutic strategy for the treatment of acute liver failure and inborn metabolic defects of the liver. Although minimally invasive, known safety risks of the method include portal vein thrombosis
Publikováno v:
Leukemia. 13:1383-1389
To analyze the value of real time RT-PCR for monitoring of bcr-abl expression in CML patients after allogeneic or autologous stem cell transplantation (SCT), we generated pairs of PCR-primers and TaqMan probes specific for either the b2a2- or the b3a
Autor:
Q Yuan, P Krause, H Christiansen, M Rave-Fränk, A Schneider, S Kafert-Kasting, H Kriegbaum, M Ott, J Meyburg, S König
Publikováno v:
Zeitschrift für Gastroenterologie. 47
Autor:
S. Kafert-Kasting, Hans Christiansen, Q. Yuan, Jochen Meyburg, Michael Ott, Margret Rave-Fränk, A. Schneider, H. Kriegbaum, Petra Krause, S. König
Publikováno v:
Deutsche Gesellschaft für Chirurgie ISBN: 9783642006241
Introduction: Hepatocyte transplantation is regarded as a promising option to correct hereditary metabolic liver disease. This study describes a novel method involving transient and regional ischaemic damage in combination with external beam irradiat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37d0fa1bad0cc797bc6232a0e1518f10
https://doi.org/10.1007/978-3-642-00625-8_62
https://doi.org/10.1007/978-3-642-00625-8_62
Autor:
Michael Ott, Q. Yuan, Petra Krause, S. Kafert-Kasting, H. Kriegbaum, Sarah König, Jochen Meyburg
Publikováno v:
Zeitschrift für Gastroenterologie. 46
Autor:
S, Hermann, F, Schestag, A, Polten, S, Kafert, J, Penzien, J, Zlotogora, N, Baumann, V, Gieselmann
Publikováno v:
American journal of medical genetics. 91(1)
Metachromatic leukodystrophy is a lysosomal storage disease caused by the deficiency of arylsulfatase A. Here we describe a hitherto unknown arylsulfatase A allele carrying a E312D missense mutation and characterize the effects of this and three prev
Publikováno v:
The Journal of biological chemistry. 274(46)
To analyze the function of each subunit of the receptor for granulocyte-macrophage colony-stimulating factor (GM-CSF), GMR, we previously generated a single-chain chimeric receptor by fusion of the extracellular and transmembrane domain from the alph